Cocconcelli P S, Gasson M J, Morelli L, Bottazzi V
Istituto di Microbiologia, Università Cattolica del Sacro Cuore, Piacenza, Italy.
Res Microbiol. 1991 Jul-Aug;142(6):643-52. doi: 10.1016/0923-2508(91)90077-n.
Vector plasmids were constructed by ligating chloramphenicol and erythromycin resistance genes to TaqI-digested DNA of a cryptic plasmid from Lactobacillus plantarum. The minimal region of Lactobacillus plasmid DNA that was required for DNA replication was defined and a single-stranded DNA intermediate replication system was observed. Homologies with other origins of replication of plasmids from Gram-positive bacteria, replicating via rolling circle mechanism, were found. It was shown that the constructed vectors, named pPSC20 and pPSC22, were transformable into L. plantarum, Lactobacillus acidophilus, Lactobacillus reuteri, Lactobacillus fermentum, Lactobacillus helveticus, Lactococcus lactis subsp. lactis, Bacillus subtilis, and Escherichia coli. Using plasmid pPSC22, the alpha-amylase gene of Bacillus stearothermophilus was cloned and expressed in several Lactobacillus species.
通过将氯霉素和红霉素抗性基因连接到植物乳杆菌隐秘质粒经TaqI酶切的DNA上构建载体质粒。确定了乳酸杆菌质粒DNA复制所需的最小区域,并观察到单链DNA中间复制系统。发现与革兰氏阳性菌中通过滚环机制复制的其他质粒复制起点存在同源性。结果表明,构建的载体pPSC20和pPSC22可转化到植物乳杆菌、嗜酸乳杆菌、罗伊氏乳杆菌、发酵乳杆菌、瑞士乳杆菌、乳酸乳球菌乳酸亚种、枯草芽孢杆菌和大肠杆菌中。利用质粒pPSC22,嗜热脂肪芽孢杆菌的α-淀粉酶基因被克隆并在几种乳酸杆菌中表达。